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Reversible Addition-Fragmentation Chain Transfer-Mediated Amphiphilic Copolymeric Composite as a Nanocarrier for Drug Delivery Application

IR@CGCRI: CSIR-Central Glass and Ceramic Research Institute, Kolkata

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Title Reversible Addition-Fragmentation Chain Transfer-Mediated Amphiphilic Copolymeric Composite as a Nanocarrier for Drug Delivery Application
 
Creator Das Karmakar, Puja
Pal, Aniruddha
Bodhak, Subhadip
Pal, Sagar
 
Subject Engineering Materials
 
Description Magnetic core-shell nanoparticle (NP)-polymer-based composite materials, in which the stimuli-responsive polymer acts as a suitable shell, become more advantageous as nanocarriers. Here, nanocomposites comprising magneto-responsive gamma-Fe2O3 NPs that incorporated amphiphilic copolymers have been synthesized. At first, the copolymer dextran grafted with poly(N-vinyl caprolactam)] has been prepared via reversible addition-fragmentation chain transfer polymerization followed by ex situ incorporation of gamma-Fe(2)O(3 )NPs. The copolymerization is living in nature as apparent from molecular weight distribution (determined using advanced polymer chromatography, i.e., APC analysis) and the reaction kinetics study. The developed nanocomposite exhibits regular core-shell morphology, where the magnetic NPs have been found to behave as the core, while the copolymer represents as the shell, as obvious from field emission scanning electron microscopy and high-resolution transmission electron microscopy analyses. The nanocarrier is non-cytotoxic and has further been studied for its effectivity as an efficient carrier for a hydrophobic drug (naproxen).
 
Date 2021-11
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://cgcri.csircentral.net/5281/1/puja.pdf
Das Karmakar, Puja and Pal, Aniruddha and Bodhak, Subhadip and Pal, Sagar (2021) Reversible Addition-Fragmentation Chain Transfer-Mediated Amphiphilic Copolymeric Composite as a Nanocarrier for Drug Delivery Application. ACS APPLIED POLYMER MATERIALS, 3 (11). pp. 5386-5396. ISSN 2637-6105
 
Relation http://cgcri.csircentral.net/5281/